Canonical Allele Identifier: CA907868589

Gene: MST1

Linked Data

• dbSNP Id: rs1486607002
• gnomAD v3: 3-49684019-A-C
• gnomAD v4: 3-49684019-A-C
• MyVariant Identifiers: chr3:g.49721452A>C (hg19) ; chr3:g.49684019A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49684019A>C , CM000665.2:g.49684019A>C	GRCh38
NC_000003.11:g.49721452A>C , CM000665.1:g.49721452A>C	GRCh37
NC_000003.10:g.49696456A>C	NCBI36
NG_011438.1:g.15018A>C
NG_016454.1:g.9745T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000449682.3:c.*9T>G MANE Select	ENSP00000414287.2:n.*9T>G
ENST00000448220.5:c.595T>G
ENST00000449682.2:c.*9T>G	ENSP00000414287.2:n.*9T>G
ENST00000479115.5:n.2242T>G
ENST00000488350.6:n.4109T>G
ENST00000492329.5:n.1963T>G
NM_020998.3:c.*9T>G	NP_066278.3:n.*9T>G
XM_006713166.1:c.*9T>G	XP_006713229.1:n.*9T>G
XM_011533730.1:c.*9T>G	XP_011532032.1:n.*9T>G
XM_011533731.1:c.*9T>G	XP_011532033.1:n.*9T>G
XM_011533732.1:c.*9T>G	XP_011532034.1:n.*9T>G
XM_011533733.1:c.*107T>G	XP_011532035.1:n.*107T>G
XR_427270.2:n.3119T>G
XR_427271.1:n.3070T>G
XR_427273.1:n.2975T>G
XR_427274.2:n.3020T>G
XR_940425.1:n.3115T>G
XR_940426.1:n.3155T>G
XR_940427.1:n.3020T>G
NR_146060.1:n.2140T>G
XM_006713166.2:c.*9T>G	XP_006713229.1:n.*9T>G
XM_011533732.2:c.*9T>G	XP_011532034.1:n.*9T>G
XM_017006460.2:c.*9T>G	XP_016861949.1:n.*9T>G
XM_017006461.2:c.*9T>G	XP_016861950.1:n.*9T>G
XM_017006462.2:c.*107T>G	XP_016861951.1:n.*107T>G
XM_017006463.2:c.*107T>G	XP_016861952.1:n.*107T>G
XM_017006464.2:c.*107T>G	XP_016861953.1:n.*107T>G
XR_001740149.2:n.2287T>G
XR_001740150.2:n.2284T>G
XR_001740151.2:n.2327T>G
XR_001740152.2:n.2242T>G
XR_001740153.2:n.2288T>G
XR_002959536.1:n.2242T>G
XR_427273.2:n.2246T>G
XR_940427.2:n.2291T>G
NM_001393581.1:c.*9T>G	NP_001380510.1:n.*9T>G
NM_001393582.1:c.*9T>G	NP_001380511.1:n.*9T>G
NM_001393583.1:c.*9T>G	NP_001380512.1:n.*9T>G
NM_001393584.1:c.*9T>G	NP_001380513.1:n.*9T>G
NM_001393585.1:c.*9T>G	NP_001380514.1:n.*9T>G
NM_020998.4:c.*9T>G MANE Select	NP_066278.3:n.*9T>G
NR_146060.2:n.2851T>G